JPS60191447A - Optical disk - Google Patents

Optical disk

Info

Publication number
JPS60191447A
JPS60191447A JP59047799A JP4779984A JPS60191447A JP S60191447 A JPS60191447 A JP S60191447A JP 59047799 A JP59047799 A JP 59047799A JP 4779984 A JP4779984 A JP 4779984A JP S60191447 A JPS60191447 A JP S60191447A
Authority
JP
Japan
Prior art keywords
fluoroalkyl
meth
polymer
acrylate
parts
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP59047799A
Other languages
Japanese (ja)
Inventor
Tetsuya Takanaga
高永 哲也
Masashi Nakamura
正志 中村
Shinobu Ikeno
池野 忍
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Electric Works Co Ltd
Original Assignee
Matsushita Electric Works Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Works Ltd filed Critical Matsushita Electric Works Ltd
Priority to JP59047799A priority Critical patent/JPS60191447A/en
Publication of JPS60191447A publication Critical patent/JPS60191447A/en
Pending legal-status Critical Current

Links

Classifications

    • GPHYSICS
    • G11INFORMATION STORAGE
    • G11BINFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
    • G11B7/00Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
    • G11B7/24Record carriers characterised by shape, structure or physical properties, or by the selection of the material
    • G11B7/241Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
    • G11B7/252Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
    • G11B7/253Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates

Abstract

PURPOSE:To obtain an optical disk which decreases warpage and twist in highly moiste environment and has excellent double refractivity and transparency by using a base material consisting of a polymer formed by polymerizing the fluoroalkyl (meth)acrylate expressed by the specific constitutional formula as an essential raw material. CONSTITUTION:A polymer obtd. by polymerizing the fluoroalkyl (meth)acrylate expressed by the formula I as an essential material is formed as a base material. Z is preferably incorporated in the form of CH2 in the fluoroalkyl (meth)acrylate to be used as the essential raw material. More specifically, the fluoroalkyl methacrylate is more preferable to the fluoroalkyl acrylate and the polymer having the higher glass transition temp. Tg and better heat resistance is obtainable with the Z incorporated in the form of CH3. The better result is obtd. as y is smaller in a 0-4 range in order to satisfy both of the glass transition point and water absorptivity. Rf may be n-alkyl, alicyclic alkyl, etc. and more preferably a branched alkyl. The better result is obtd. as the C is larger within a 1-20 range.

Description

【発明の詳細な説明】 〔技術分野〕 この発明は、レーザー光の反射または透過により記録さ
れた信号の読み出しを行う光学式情報記録用ディスクに
関する。
DETAILED DESCRIPTION OF THE INVENTION [Technical Field] The present invention relates to an optical information recording disc that reads recorded signals by reflection or transmission of laser light.

〔背景技術〕[Background technology]

現在一般に用いられている光学式ディスクは、メチルメ
タクリレートを主成分としているため、特に、多湿環境
に置かれた際に反りやネジレが発生しやすい。反りやネ
ジレの発生は、記録情報の適確な再生に大きな障害とな
る。そこで、吸水性を改良して反りやネジレの発生を少
なくするため、スチレンをメチルメタクリレートと共重
合させることが行われる。しかし、スチレンを多く共重
合させると、今度は、複屈折が大きくなってくるという
問題が新たに生じてくる。
Optical discs currently in common use contain methyl methacrylate as a main component, and are therefore susceptible to warping and twisting, especially when placed in humid environments. The occurrence of warpage and twisting becomes a major hindrance to accurate reproduction of recorded information. Therefore, in order to improve water absorption and reduce the occurrence of warping and twisting, styrene is copolymerized with methyl methacrylate. However, when a large amount of styrene is copolymerized, a new problem arises in that birefringence increases.

〔発明の目的〕[Purpose of the invention]

この発明は、このような事情に鑑みてなされたもので、
多湿環境下でも反りやネジレの発生が少なく、しかも、
複屈折性や透明性にも優れた光学式ディスクを提供する
ことを目的としている。
This invention was made in view of these circumstances,
It is less likely to warp or twist even in a humid environment, and
The objective is to provide an optical disc with excellent birefringence and transparency.

〔発明の開示〕[Disclosure of the invention]

前記のような目的を達成するため、発明者らは、まず、
フルオロ(メタ)アクリレートを必須原材料として重合
させた重合体を基材として用いることに着目した。フル
オロ(メタ)アクリレートを必須原材料とした理由は、
光線透過率が高く、複屈折が小さいというポリ(メタ)
アクリル酸エステルの長所を生かすようにして、その欠
点である吸水性および耐熱性が劣ることを、フッ素置換
による溌水性の向上と、分子間結合力の強化とにより改
善することができるからである。一般に、ポリ(メタ)
アクリル酸エステルは、フッ素置換することによりガラ
ス転移温度が数十度も高くなって耐熱性が向肥し、吸水
率も大巾に低下する。発明者らは、さらに、研究を重ね
た結果、光学式ディスクに用いるのに適した種類のフル
オロ(メタ)アクリレートを見出し、ここにこの発明を
完成した。
In order to achieve the above objectives, the inventors first
We focused on using a polymer made by polymerizing fluoro(meth)acrylate as an essential raw material as a base material. The reason why fluoro(meth)acrylate was selected as an essential raw material is
Poly(meta) has high light transmittance and low birefringence.
This is because by taking advantage of the advantages of acrylic ester, its disadvantages of poor water absorption and heat resistance can be improved by improving water repellency through fluorine substitution and strengthening intermolecular bonding strength. . In general, poly(meta)
When acrylic acid ester is substituted with fluorine, its glass transition temperature increases by several tens of degrees, improving its heat resistance and significantly reducing its water absorption. As a result of further research, the inventors discovered a type of fluoro(meth)acrylate suitable for use in optical discs, and have now completed this invention.

したがって、この発明は、下記の構造式であられされる
フルオロアルキル(メタ)アクリレートを必須原材料と
して重合させた重合体を基材とする光学式ディスクをそ
の要旨としている。
Therefore, the gist of the present invention is an optical disk whose base material is a polymer obtained by polymerizing fluoroalkyl (meth)acrylate represented by the following structural formula as an essential raw material.

1 RtCCH2’)y−0−C−C=CH2Z ; CH
3またばH y;0〜4 Rf;フルオロアルキル基で炭素数カ1〜20のもの 以下に、この発13j4を詳しく説明する。
1 RtCCH2')y-0-C-C=CH2Z; CH
3 or H y; 0-4 Rf; fluoroalkyl group having 1 to 20 carbon atoms This expression 13j4 will be explained in detail below.

ここで、必須原材料として用いられる前記式のフルオロ
アルキル(メタ)アクリレートは、ZがCH3となって
いるのが好ましい。すなわち、フルオロアルキルメタク
リレートの方がフルオロアルキルアクリレートよりも好
ましい。2がCH3となっている方がガラス転移温度(
Tg )が高く、耐熱性の優れた重合体が得られるから
である。ところで、カラス転移点は、エステルのアルコ
ール成分Rt (CH2)y−の分岐(指環も含む)が
多い程、また炭素数が少ない程高くなる。他方、吸水率
は、yを小さくし、R,の炭素数全多くして重合体中の
フッ素含量を高くすると低くなる。そこで、ガラス転移
点および吸水率の両方を満足させるには、yは0〜4の
範囲において、小さい方が好ましく、RtIdn−アル
キル、脂環式アルキル等でもよいが、分岐アルキルとな
っているのが好1しく、炭素数は1〜20の範囲内にお
いて多い方が好ましい。
Here, in the fluoroalkyl (meth)acrylate of the above formula used as an essential raw material, Z is preferably CH3. That is, fluoroalkyl methacrylate is more preferred than fluoroalkyl acrylate. The glass transition temperature (
This is because a polymer having a high Tg) and excellent heat resistance can be obtained. Incidentally, the Callus transition point increases as the number of branches (including a ring) of the alcohol component Rt (CH2)y- of the ester increases and as the number of carbon atoms decreases. On the other hand, the water absorption rate decreases when y is decreased and the total number of carbon atoms in R is increased to increase the fluorine content in the polymer. Therefore, in order to satisfy both the glass transition point and the water absorption rate, y is preferably smaller in the range of 0 to 4, and may be RtIdn-alkyl, alicyclic alkyl, etc., but branched alkyl is preferable. is preferred, and the number of carbon atoms is preferably as large as 1 to 20.

さらに、完全置換されてパーフルオロアルキル基となっ
ているのが好ましい。Rr(Cfh)y−としてみると
、炭素数が:)〜8で分岐しているのが好ましい。たと
えば、下記の式であられされるもの等が好ましい例とし
てあげられる。
Furthermore, it is preferable that the group is completely substituted to become a perfluoroalkyl group. When viewed as Rr(Cfh)y-, it is preferable that the number of carbon atoms is :) to 8 and branched. For example, preferred examples include those represented by the following formula.

フルオロアルキル(メタ)アクリレート単独で重合させ
てなるポリフルオロアルキル(メタ)了クリレート(ホ
モポリマー)を基材として用いてもよいが、この発明の
目的を阻害しない範囲において、1種以上の他の単量体
との共重合体を基材として用いてもよい。この場合、フ
ルオロアルキル(メタ)アクリレートの使用割合はでき
るだけ多いのがよい。他の単量体としては、たとえば、
(メタ)アクリル酸エステル、その他のビニル系単量体
が好ましく用いられる。(メタ)アクリル酸エステルと
しては、分岐(メタ)アクリル酸エステルを用いるのが
好ましい。他のビニル系単量体トシてハ、ビニルトルエ
ン、エチルスチレン、イソプロピルスチレン、 i −
フチルステレン、p−ノナルスナレン等が用いられるが
、熱分解温度の萬いp−メチルスチレンを用いるのが好
ましい。
Polyfluoroalkyl (meth)acrylate (homopolymer) obtained by polymerizing fluoroalkyl (meth)acrylate alone may be used as a base material, but one or more other types may be used as long as the purpose of the present invention is not impaired. A copolymer with a monomer may be used as the base material. In this case, it is preferable that the proportion of fluoroalkyl (meth)acrylate used be as high as possible. Other monomers include, for example,
(Meth)acrylic acid esters and other vinyl monomers are preferably used. As the (meth)acrylic ester, it is preferable to use a branched (meth)acrylic ester. Other vinyl monomers, vinyltoluene, ethylstyrene, isopropylstyrene, i-
Phylsterene, p-nonalsunarene, etc. are used, but it is preferable to use p-methylstyrene, which has a thermal decomposition temperature.

フルオロアルキル(メタ)アクリレート、(メタ)アク
リル酸エステルおよび必要に応じて両者以外のビニル系
tu社体を共重合させる場合は、フルオロアルギル(ツ
タ)アクリレート80〜20M量部、(メタ)アクリル
酸エヌテル10〜50重量部9両者以外のビニル系単量
体を0〜40重量部の割合で合計100重は部の単量体
を共重合させるようにするのが好ましい。
When copolymerizing fluoroalkyl (meth)acrylate, (meth)acrylic acid ester, and, if necessary, a vinyl-based product other than both, 80 to 20 M parts of fluoroalkyl (ivy) acrylate, (meth)acrylic It is preferable to copolymerize 10 to 50 parts by weight of the vinyl monomers other than Acid Nether and 9 to 40 parts by weight in a total of 100 parts by weight.

重合体は、例えば塊状重合去、懸濁車合法、溶液重合法
、乳化重合法等の公知の重合体製造法のいずれの方法に
よって製造されてもよい。
The polymer may be produced by any of the known polymer production methods, such as bulk polymerization, suspension wheel method, solution polymerization method, and emulsion polymerization method.

基材の成分として、スタンパ−との離型性を改良する目
的で、例えばシリコン、ワックス、脂肪酸、脂肪酸エス
テル、脂肪酸金属塩、脂肪族アルコール等の助剤や、帯
電防止の目的で、例えば高級アルコールのヌルフオン酸
塩、第+級アンモニウム塩等の助剤をこの発明の目的の
達成を阻害しない範囲で、上記の重合体に併用してもよ
い。
The components of the base material include auxiliary agents such as silicone, wax, fatty acids, fatty acid esters, fatty acid metal salts, and aliphatic alcohols for the purpose of improving mold releasability from the stamper, and high-grade additives for the purpose of preventing static electricity. Auxiliary agents such as alcohol nurfonic acid salts and +-class ammonium salts may be used in combination with the above-mentioned polymers to the extent that they do not impair the achievement of the objects of the present invention.

この発明の光学式ディヌクを製造するにあたっては、た
とえばつぎのようにして行う。まず、重合体を射出成型
または直圧成型等の方法によって、ヌタンバーをセット
した金型により記録信号となるピットを転写しディスク
基材を成形する。成形はできるだけ残留応力が小さくな
るような条件で行う必要がある。つぎに、複製ディスク
の場合には一般的には、ビット転写面に金楓の真空蒸着
、スパッタリングあるいはイオンブレーティング等の方
法によって反射層を形成し、さらに必要に応じて反射層
の保護コーティングを行って製造することができる。ま
た、メモリーディヌクの場合には上記と同様にしてトラ
ッキング信号となるビットを転写した後、さらにビット
面に、例えば非晶質レアーメタルやレーザーによって熱
的に分解し得る化合物のユーザーでの書き込み可能な記
録層全蒸着または塗布し、さらに必要に応じ上記のよう
な反射層や保護コーティングの形成を行ってメモリー用
光学式ディスクを製造することができる。
The optical Dinuk of the present invention is manufactured, for example, in the following manner. First, a method such as injection molding or direct pressure molding of a polymer is used to transfer pits, which will become recording signals, using a mold set with nutanvar to form a disk base material. Molding must be performed under conditions that minimize residual stress. Next, in the case of a duplicate disc, a reflective layer is generally formed on the bit transfer surface by vacuum deposition of gold maple, sputtering, or ion blasting, and if necessary, a protective coating for the reflective layer is applied. You can go and manufacture it. In addition, in the case of Memory Dinuk, after transferring the bit that becomes the tracking signal in the same manner as above, it is possible for the user to write on the bit surface with, for example, amorphous rare metals or compounds that can be thermally decomposed by laser. An optical disk for memory can be manufactured by fully depositing or coating a recording layer, and further forming a reflective layer or a protective coating as described above, if necessary.

前記のようにして得られるこの発明の光学式ディスクは
、フルオロアルキル(メタ)アクリレートを必須原材料
とする重合体が基材として用いられているので、メチル
メタクリレートを主原材料とするポリメチルメタクリレ
ート(PΔ(MA)等の重合体が基材として用いられて
いるものに比べ、吸水率が小さくなる。普通、0.20
4程度以下となる。
Since the optical disc of the present invention obtained as described above uses a polymer containing fluoroalkyl (meth)acrylate as an essential raw material as a base material, polymethyl methacrylate (PΔ Compared to those using polymers such as (MA) as the base material, the water absorption rate is lower. Usually 0.20
It will be about 4 or less.

そのため、多湿による反りゃネジレの発生が非常に少な
い。そのうえ、光学的に均質で複屈折性に優れ、透明性
にも優れている。また、この発明で用いられる重合体は
、普通、ガラス転移温度が70℃程度以上となるので、
熱による反りゃネジレ等の変形も生じにぐいものになる
Therefore, there is very little chance of warping or twisting due to high humidity. Furthermore, it is optically homogeneous, has excellent birefringence, and has excellent transparency. Furthermore, since the polymer used in this invention usually has a glass transition temperature of about 70°C or higher,
Warping due to heat also causes deformation such as twisting.

つぎに、実施例について説明する。Next, examples will be described.

(実施例1) IEのセバラプルフラヌコに、下記の原材料全仕込んだ
。ただし、部は重量部をあられすものとする。
(Example 1) All of the following raw materials were charged into IE's Sebara Purfuranuco. However, parts are by weight.

10 ) (フルオロアルキルツタクリレート)1 i蒸留水(ヒ
ドロキシエチルセルロースを0.5重量係含有)3 部
過酸化ベンゾイル 0.015部 n−ラウリルメルカプタン 0.005i撹拌速度20
0rpm、浴温80℃で、3〜4時間重合反応させた。
10) (Fluoroalkyl tacrylate) 1 i Distilled water (contains 0.5 weight percent of hydroxyethyl cellulose) 3 parts Benzoyl peroxide 0.015 parts n-lauryl mercaptan 0.005 i Stirring speed 20
The polymerization reaction was carried out at 0 rpm and a bath temperature of 80° C. for 3 to 4 hours.

重合終了後、重合体を70メツシユのステンレスふるい
でふるいにかけ、熱水で洗浄した。つぎに、減圧乾燥器
内に重合体を移し、80℃、lmmHgの条件で24時
間乾燥して、ポリマーピーズを得た。
After the polymerization was completed, the polymer was sieved through a 70-mesh stainless steel sieve and washed with hot water. Next, the polymer was transferred into a vacuum dryer and dried at 80° C. and 1 mmHg for 24 hours to obtain polymer beads.

このポリマービーズを用いてディスク基材を成形した。A disk base material was molded using the polymer beads.

つぎに、ディスク基材に反射層を形成し、反射1−の保
護コーティングを行って光学式ディヌ □りをつくった
Next, a reflective layer was formed on the disc base material, and a protective coating of Reflection 1- was applied to create an optical disc.

(実施例2,3) フルオロアルキルツタクリレートトシて、下記の式であ
られされるものをそれぞれ使用するよう(10) にしたほかは、実施例1と同じようにして、ポリマービ
ーズをつくり、光学式ディスクをつくった。
(Examples 2 and 3) Polymer beads were made in the same manner as in Example 1, except that fluoroalkyl ivy acrylate was used as expressed by the following formula (10). Created an optical disc.

(実施例4) フルオロアルキルメタクリレートとして、ツタクリル酸
エステルとして、 MMA(メチルメタクリレート) 40部ビニルモノマ
ーとして、 p−メナルスナレン 20部 をそれぞれ用いて、実施例1と同じ反応条件で重合反応
を行ってポリマービーズをつくり、さらに光学式ディス
クをつくった。
(Example 4) A polymerization reaction was carried out under the same reaction conditions as in Example 1 using fluoroalkyl methacrylate, tutaacrylic acid ester, 40 parts of MMA (methyl methacrylate), and 20 parts of p-menalsunarene as a vinyl monomer. They made beads and then optical discs.

(実施例5) H3O 1II CHz=C−C−0−CHz−(CFz)3−CF3I
 15部MMA(メチルメタクリレート) 35部p−
メチルスナレン 15部 上記の原材料を用いて、実施例1と同じ反応条件で重合
反応を行ってポリマービーズをつくり、さらに光学式デ
ィヌクをつくった。
(Example 5) H3O 1II CHz=C-C-0-CHz-(CFz)3-CF3I
15 parts MMA (methyl methacrylate) 35 parts p-
Methylsunarene 15 parts Using the above-mentioned raw materials, a polymerization reaction was carried out under the same reaction conditions as in Example 1 to produce polymer beads, and further, optical Dinuk was produced.

実施例1〜5で得られた重合体につき、ガラス転移温度
および吸水率を測定し、ディスク基材につき複屈折の有
無を調べ、光学式ディスクにつき、多湿環境下における
反り、ネジレの発生の難易を調べた。ただし、ガラス転
移温度は、粘弾性ヌペクトロノーターを用いて温度分散
測定ケ行ない、動的損失(振動数10H,)がピークを
示す時の温度を取った。吸水率は、JIS K691i
に従い、23士2℃の蒸留水に24時間浸漬した後の値
を取った。複屈折の有無は、光学式ディヌクの製造過程
において反射層形成前に東京光学機械株式会社製ノの5
train Viewerを用い、着色度合(干渉しま
)を観察することによって判定した。反り、ネジレの発
生の難易は、45℃、相対湿度95優の環境下に光学式
7デイスク(反射層及び保護コートを施したもの)を放
置した後の反り、ネジレの発生の有無を調べることによ
り判定した。結果を第1表に示す。
The glass transition temperature and water absorption rate of the polymers obtained in Examples 1 to 5 were measured, and the presence or absence of birefringence of the disk base material was investigated. I looked into it. However, the glass transition temperature was determined by temperature dispersion measurement using a viscoelastic nupectronator, and the temperature at which the dynamic loss (frequency: 10 H) reached its peak was taken. Water absorption rate is JIS K691i
According to the above, the values were taken after immersion in distilled water at 2°C for 24 hours. The presence or absence of birefringence is determined by measuring the presence or absence of birefringence using the Tokyo Kogaku Kikai Co., Ltd.
The determination was made by observing the degree of coloring (interference stripes) using a train viewer. To determine whether or not warping or twisting occurs, check whether or not warping or twisting occurs after leaving an optical 7 disc (with a reflective layer and protective coating) in an environment of 45°C and relative humidity of 95%. Judgment was made by The results are shown in Table 1.

第 1 表 第1表より、実施例1〜5の光学式ディスクは、使用し
た重合体のガラス転移温度が高いので、熱による反りや
ネジレ等の変形を生じにくく、吸水率が小さいので、多
湿環境下において反りゃネジレが発生せず、複屈折も起
こさないことがわかる。
Table 1 From Table 1, the optical discs of Examples 1 to 5 have high glass transition temperatures of the polymers used, so they are less prone to deformation such as warping or twisting due to heat, and have low water absorption, so they can be used in high humidity. It can be seen that no torsion occurs when the material is warped in the environment, and no birefringence occurs.

〔発明の効果〕〔Effect of the invention〕

この発明にかかる光学式ディスクは、前記一般式であら
れされる構造のフルオロアルキル(メタ)アクリレート
を必須原材料として重合させた重合体を基材とするので
、多湿環境ドでも反りゃネジレの発生が少なく、しかも
、複屈折性や透明性にも優れている。
Since the optical disc according to the present invention is made of a polymer obtained by polymerizing fluoroalkyl (meth)acrylate having the structure represented by the above general formula as an essential raw material, it will not warp or twist even in a humid environment. Moreover, it has excellent birefringence and transparency.

代理人 弁理士 松 本 武 彦 零[糸六ネ甫正書(自発) 昭和59年 6月 4日 2、発明の名称 光学式ディスク 3、補正をする者 事件との関係 特許出願人 柱 所 大阪府門真市大字門真1048番地名 称(5
83)松下電工株式会社 代表者 代表輔役 小 林 郁 4、代理人 6、補正の対象 明細書 7、補正の内容 (1)明細書の特許請求の範囲面の全文を別紙のとおり
に訂正する。
Agent Patent Attorney Takehiko Rei Matsumoto [Ito Roku Neho Seisho (Spontaneous) June 4, 1981 2 Name of the invention Optical Disk 3 Relationship with the person making the amendment Case Patent applicant Location Osaka Prefecture 1048 Kadoma, Kadoma City Name (5)
83) Matsushita Electric Works Co., Ltd. Representative Representative: Iku Kobayashi 4, Agent 6, Specification subject to amendment 7, Contents of amendment (1) The entire text of the scope of claims of the specification will be corrected as shown in the attached sheet. .

(2) 〔補正後の特許請求の範囲〕 2、特許請求の範囲 (1)下記の構造式であられされるフルオロアルキル(
メタ)アクリレートを必須原材料として重合させた重合
体を基材とする光学式ディスク。
(2) [Claims after amendment] 2. Scope of claims (1) Fluoroalkyl (
An optical disc whose base material is a polymer made by polymerizing meth)acrylate as an essential raw material.

Z ; CH3またはH y;0〜4 Rf、フルオロアルキル基で炭素数が1〜20のもの (2)重合体が、フルオロアルキル(メタ)アクリレー
ト80〜20重量部、 (メタ)アクリル酸エステル1
0〜50重量部2両者以外のビニル系単量体0〜40重
量部の割合でそれぞれ含む合計100重量部の単量体が
共重合してなる共重合体である特許請求の範囲第1項記
載の光学式ディスク。
Z; CH3 or H y; 0-4 Rf, fluoroalkyl group with 1-20 carbon atoms (2) The polymer contains 80-20 parts by weight of fluoroalkyl (meth)acrylate, (meth)acrylic acid ester 1
Claim 1 which is a copolymer formed by copolymerizing 100 parts by weight of vinyl monomers other than both in a proportion of 0 to 50 parts by weight, respectively. Optical disc as described.

〔3) メタクリル酸エステルがメチルメタクリレート
、ビニル系単量体がアルキル置換スチレンである特許請
求の範囲第2項記載の光学式ディスク(4)重合体が、
ガラス転移温度70℃以上、吸水率0.20%以下であ
る特許請求の範囲第1項から第3項までのいずれかに記
載の光学式ディスク。
[3] The optical disk (4) polymer according to claim 2, wherein the methacrylic acid ester is methyl methacrylate and the vinyl monomer is alkyl-substituted styrene,
The optical disc according to any one of claims 1 to 3, having a glass transition temperature of 70° C. or more and a water absorption rate of 0.20% or less.

9191

Claims (3)

【特許請求の範囲】[Claims] (1) 下記の構造式であられされるフルオロアルキル
(メタ)アクリレートを必須原材料として重合させた重
合体を基材とする光学式ディスク。 Z;CH3またはH y;0〜4 Rf;フルオロアルキル基で炭素数が1〜20のもの
(1) An optical disc whose base material is a polymer obtained by polymerizing fluoroalkyl (meth)acrylate having the following structural formula as an essential raw material. Z; CH3 or H y; 0-4 Rf; fluoroalkyl group with 1-20 carbon atoms
(2)重合体が、フルオロアルキル(メタ)アクIJL
/−ト80〜20重f部、(メタ)アクリル酸エステル
10〜50重量部9両者以外のビニル系単量体0〜40
重量部の割合でそれぞれ含む合計1007ijd部の単
量体が共重合してなる共重合体である特許請求の範囲第
1項記載の光学式ディスク。
(2) The polymer is fluoroalkyl (meth)ac IJL
/-t 80-20 parts by weight, (meth)acrylic acid ester 10-50 parts by weight 9 Vinyl monomers other than both 0-40
2. The optical disc according to claim 1, which is a copolymer formed by copolymerizing a total of 1007 ijd parts of each monomer in a proportion of parts by weight.
(3)メタクリル酸エステルがメチルメタクリレート、
ヒニル系単を体がアルキル置換スチレンである特許請求
の範囲第2項記載の光学式ディスク(4)重合体が、ガ
ラス転移温度70℃以上2.吸水率0.20’ %以上
である特許請求の範囲第1項から第3項までのいずれか
に記載の光学式ディスク。
(3) Methacrylic acid ester is methyl methacrylate,
2. The optical disk (4) polymer according to claim 2, wherein the hynyl monomer is an alkyl-substituted styrene, has a glass transition temperature of 70° C. or more. The optical disc according to any one of claims 1 to 3, which has a water absorption rate of 0.20'% or more.
JP59047799A 1984-03-12 1984-03-12 Optical disk Pending JPS60191447A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP59047799A JPS60191447A (en) 1984-03-12 1984-03-12 Optical disk

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP59047799A JPS60191447A (en) 1984-03-12 1984-03-12 Optical disk

Publications (1)

Publication Number Publication Date
JPS60191447A true JPS60191447A (en) 1985-09-28

Family

ID=12785414

Family Applications (1)

Application Number Title Priority Date Filing Date
JP59047799A Pending JPS60191447A (en) 1984-03-12 1984-03-12 Optical disk

Country Status (1)

Country Link
JP (1) JPS60191447A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989005287A1 (en) * 1987-12-04 1989-06-15 Daikin Industries, Ltd. Hexafluoroneopentyl alcohol, its derivatives, fluorinated polymers and their use
US5175790A (en) * 1989-04-13 1992-12-29 Hoechst Aktiengesellschaft Transparent thermoplastic molding compound made of 2,3-difluoroacrylic acid esters
US5223593A (en) * 1991-08-08 1993-06-29 Minnesota Mining And Manufacturing Company Fluorine containing plastic optical fiber cores
US5288825A (en) * 1990-03-29 1994-02-22 Mitsubishi Rayon Company Ltd. Fluoroacrylic polymer having lubricating effect and thermoplastic resin composition comprising same
JP2009233932A (en) * 2008-03-26 2009-10-15 Toshiba Tec Corp Tractor

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989005287A1 (en) * 1987-12-04 1989-06-15 Daikin Industries, Ltd. Hexafluoroneopentyl alcohol, its derivatives, fluorinated polymers and their use
US5175790A (en) * 1989-04-13 1992-12-29 Hoechst Aktiengesellschaft Transparent thermoplastic molding compound made of 2,3-difluoroacrylic acid esters
US5283303A (en) * 1989-04-13 1994-02-01 Hoechst Aktiengesellschaft Transplant thermoplastic molding compound made of 2,3-difluoroacrylic acid esters
US5288825A (en) * 1990-03-29 1994-02-22 Mitsubishi Rayon Company Ltd. Fluoroacrylic polymer having lubricating effect and thermoplastic resin composition comprising same
US5223593A (en) * 1991-08-08 1993-06-29 Minnesota Mining And Manufacturing Company Fluorine containing plastic optical fiber cores
JP2009233932A (en) * 2008-03-26 2009-10-15 Toshiba Tec Corp Tractor

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